Canonical Allele Identifier: PA281970
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40367
ClinVar RCV Id: RCV000033308 RCV000417719 RCV000654957 RCV002051798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Val471Phe
CA281968
NM_004333.6:c.1411G>T