Canonical Allele Identifier: PA2828481927
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1401032
ClinVar RCV Id: RCV001911609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Ser325Cys
CA369590320
NM_001374258.1:c.974C>G