Canonical Allele Identifier: PA2828780518
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376071
ClinVar RCV Id: RCV000427646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Ile504Val
CA16602533
NM_001378475.1:c.1510A>G