Canonical Allele Identifier: PA2828780373
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 547184
ClinVar RCV Id: RCV000659285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Gln373Arg
CA369588914
NM_001378475.1:c.1118A>G