Canonical Allele Identifier: PA2827254687
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1798868
ClinVar RCV Id: RCV002435839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Ser558Asn
CA368987225
NM_001324402.2:c.1673G>A