Canonical Allele Identifier: PA2827253980
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 524880
ClinVar RCV Id: RCV000628759 RCV001013433 RCV001756034 RCV002483765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr191Ile
CA4448286
NM_001324402.2:c.572C>T