Canonical Allele Identifier: PA2828775221
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40379
ClinVar RCV Id: RCV000626038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Trp534Leu
CA281983
NM_001378467.1:c.1601G>T