Canonical Allele Identifier: PA1139743281
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 864012
ClinVar RCV Id: RCV001071102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Leu581Phe
CA369588073
NM_001374258.1:c.1741C>T