Canonical Allele Identifier: PA2580134060
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2155877
ClinVar RCV Id: RCV003090779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Thr777Ile
CA368981973
NM_001127500.3:c.2330C>T