Canonical Allele Identifier: PA123610
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_001120972.1:p.Thr1191Ile
CA123608
NM_001127500.3:c.3572C>T