Canonical Allele Identifier: PA256999
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_001120972.1:p.Val1238Ile
CA256997
NM_001127500.3:c.3712G>A