Canonical Allele Identifier: PA2828776003
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 76687
ClinVar RCV Id: RCV000431444 RCV000443326 RCV000427485 RCV000437736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Leu597Gln
CA16602257
NM_001378468.1:c.1790T>A