Canonical Allele Identifier: PA2828779239
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13961
ClinVar RCV Id: RCV000014992 RCV000014993 RCV000014994 RCV000022677 RCV000080903 RCV000037936 RCV000067669 RCV000208763 RCV000420614 RCV000425847 RCV000429915 RCV000440802 RCV000425166 RCV000430562 RCV000443745 RCV000433305 RCV000435441 RCV000440540 RCV000443448 RCV000417746 RCV000424470 RCV000432628 RCV000662278 RCV000860020 RCV001030023 RCV001248834 RCV001254874 RCV002051586 RCV004018627 RCV003458334
ClinVar Variation Id: 376069
ClinVar RCV Id: RCV000424781 RCV000442563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Val548Glu
CA123643
NM_001378473.1:c.1643T>A
CA16602531
NM_001378473.1:c.1643_1644delinsAA