Canonical Allele Identifier: PA2828775840
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13963
ClinVar RCV Id: RCV000014996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Ile463Ser
CA250634
NM_001378468.1:c.1388T>G