Canonical Allele Identifier: PA2828775836
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 547184
ClinVar RCV Id: RCV000659285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Gln461Arg
CA369588914
NM_001378468.1:c.1382A>G