Canonical Allele Identifier: PA916027578
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13885
ClinVar RCV Id: RCV000014899 RCV000441479 RCV000430628 RCV000420374 RCV001851861 RCV002362584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Tyr800Cys
CA257003
NM_001324402.2:c.2399A>G