Canonical Allele Identifier: PA281979
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40373
ClinVar RCV Id: RCV000033316 RCV000822490 RCV001089762 RCV001261045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Glu501Ala
CA281977
NM_004333.6:c.1502A>C