Canonical Allele Identifier: PA2828777299
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13979
ClinVar RCV Id: RCV000015013 RCV000033329 RCV000211751 RCV000474979 RCV003450642 RCV004018631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Asn547Asp
CA279976
NM_001378470.1:c.1639A>G