Canonical Allele Identifier: PA135097
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44813
ClinVar RCV Id: RCV000037931 RCV000417722 RCV000425110 RCV000432782 RCV000432575 RCV000440132 RCV000443573 RCV000422928 RCV000425325 RCV000434944 RCV000444338 RCV002291550
ClinVar Variation Id: 375948
ClinVar RCV Id: RCV000427497 RCV001374449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Asp594Asn
CA135095
NM_004333.6:c.1780G>A
CA16602427
NM_004333.6:c.1779_1780delinsGA