Canonical Allele Identifier: PA2828776478
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711779
ClinVar RCV Id: RCV002293324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Ser425Cys
CA369589014
NM_001378469.1:c.1273A>T