Canonical Allele Identifier: PA2827254692
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411918
ClinVar RCV Id: RCV000476062 RCV001018130 RCV001312218 RCV001788226 RCV001755706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Pro561Ser
CA4448619
NM_001324402.2:c.1681C>T