Canonical Allele Identifier: PA916027395
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 188358
ClinVar RCV Id: RCV000168390 RCV000564000 RCV000610933 RCV001507175 RCV001843487 RCV003927559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Ser572Asn
CA334713
NM_001324401.3:c.1715G>A