Canonical Allele Identifier: PA916027583
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13890
ClinVar RCV Id: RCV000014904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Lys814Arg
CA123614
NM_001324402.2:c.2441A>G