Canonical Allele Identifier: PA2828778611
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Gly544Val
CA220161
NM_001378472.1:c.1631G>T