Canonical Allele Identifier: PA645447732
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 246642
ClinVar RCV Id: RCV000236130 RCV001312219 RCV002450741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Val121Ala
CA10584669
NM_001127500.3:c.362T>C