Canonical Allele Identifier: PA2827253398
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 659496
ClinVar RCV Id: RCV000816516 RCV001015393 RCV003442109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Glu781Ala
CA4448456
NM_001324401.3:c.2342A>C