Canonical Allele Identifier: PA2828776491
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 547184
ClinVar RCV Id: RCV000659285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gln439Arg
CA369588914
NM_001378469.1:c.1316A>G