Canonical Allele Identifier: PA2827254685
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1802753
ClinVar RCV Id: RCV002466028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Arg557Gly
CA368987211
NM_001324402.2:c.1669C>G