Canonical Allele Identifier: PA645448134
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411908
ClinVar RCV Id: RCV000470541 RCV001018162 RCV002291639 RCV001837917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Thr1010Ala
CA4448620
NM_001127500.3:c.3028A>G