Canonical Allele Identifier: PA2828775999
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375943
ClinVar RCV Id: RCV000418853 RCV000421748 RCV000429106 RCV000429746 RCV000436498 RCV000439396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Gly596Arg
CA16602422
NM_001378468.1:c.1786G>C