Canonical Allele Identifier: PA916027559
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13888
ClinVar RCV Id: RCV000014902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr743Ile
CA123608
NM_001324402.2:c.2228C>T