Canonical Allele Identifier: PA1139744763
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Ser326Leu
CA135149
NM_001378467.1:c.977C>T