Canonical Allele Identifier: PA1139743271
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Leu525Ser
CA280052
NM_001374258.1:c.1574T>C