Canonical Allele Identifier: PA2828778473
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Phe416Ser
CA280002
NM_001378472.1:c.1247T>C