Canonical Allele Identifier: PA2825621153
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 3232957
ClinVar RCV Id: RCV004523589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Arg976Ile
CA368986759
NM_001127500.3:c.2927G>T