Canonical Allele Identifier: PA2825617605
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2919100
ClinVar RCV Id: RCV003764428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Val6Gly
CA164887563
NM_001127500.3:c.17T>G