Canonical Allele Identifier: PA2827253368
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1318557
ClinVar RCV Id: RCV001753332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Gly762Arg
CA368982018
NM_001324401.3:c.2284G>C