Canonical Allele Identifier: PA2573065546
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_001120972.1:p.Gly780Arg
CA368982018
NM_001127500.3:c.2338G>C