Canonical Allele Identifier: PA2828776987
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44830
ClinVar RCV Id: RCV000037958 RCV000339233 RCV000788008 RCV000824912 RCV002513490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Phe213Val
CA135140
NM_001378470.1:c.637T>G