Canonical Allele Identifier: PA916027573
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13883
ClinVar RCV Id: RCV000014897 RCV000221989 RCV001579843 RCV001376555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Val790Ile
CA256997
NM_001324402.2:c.2368G>A