Canonical Allele Identifier: PA2828776509
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1905687
ClinVar RCV Id: RCV002583696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Ser445Leu
CA168090516
NM_001378469.1:c.1334C>T