Canonical Allele Identifier: PA2828777935
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 29808
ClinVar Variation Id: 265358
ClinVar RCV Id: RCV000255590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Trp494Cys
CA250333
NM_001378471.1:c.1482G>C
CA10588419
NM_001378471.1:c.1482G>T