Canonical Allele Identifier: PA2828775695
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1709831
ClinVar RCV Id: RCV002290173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Ser314Thr
CA369590384
NM_001378468.1:c.940T>A