Canonical Allele Identifier: PA160435
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 132694
ClinVar RCV Id: RCV000119117 RCV000121345 RCV000657129 RCV001420970 RCV003467064 RCV000567774 RCV003894956 RCV003492511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ala347Thr
CA160433
NM_001127500.3:c.1039G>A