Canonical Allele Identifier: PA2827253389
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1790456
ClinVar RCV Id: RCV002457909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Val776Gly
CA368982386
NM_001324401.3:c.2327T>G