Canonical Allele Identifier: PA2828779111
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13975
ClinVar RCV Id: RCV000015009 RCV000208764 RCV000211749 RCV000680805 RCV001172276 RCV001849264 RCV003415705 RCV004018629
ClinVar Variation Id: 177844
ClinVar RCV Id: RCV000154481 RCV000844617 RCV000824921 RCV001192586 RCV003317101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Leu433Phe
CA273414
NM_001378473.1:c.1299G>C
CA280060
NM_001378473.1:c.1299G>T