Canonical Allele Identifier: PA2827254291
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 645086
ClinVar RCV Id: RCV000799105 RCV001015266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr357Ala
CA368982573
NM_001324402.2:c.1069A>G