Canonical Allele Identifier: PA2828474617
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13963
ClinVar RCV Id: RCV000014996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Ile503Ser
CA250634
NM_001374244.1:c.1508T>G