Canonical Allele Identifier: PA093813
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_000236.2:p.Thr1173Ile
CA123608
NM_000245.4:c.3518C>T