Canonical Allele Identifier: PA1139743293
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40387
ClinVar RCV Id: RCV000033332 RCV000077865 RCV000208758 RCV000431311 RCV000438697 RCV000424067 RCV000441123 RCV000844615 RCV000856749 RCV001265809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Gly636Val
CA220161
NM_001374258.1:c.1907G>T