Canonical Allele Identifier: PA1139743258
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13967
ClinVar RCV Id: RCV000015001 RCV000037916 RCV000421693 RCV000424032 RCV000429151 RCV000436576 RCV000438953 RCV000438708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Gly506Val
CA123647
NM_001374258.1:c.1517G>T