Canonical Allele Identifier: PA2827254249
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1061371
ClinVar RCV Id: RCV001370941 RCV002465868 RCV002447489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Gly332Asp
CA368982027
NM_001324402.2:c.995G>A