Canonical Allele Identifier: PA916027531
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 186141
ClinVar RCV Id: RCV000165679 RCV000443267 RCV000425188 RCV000709041 RCV001376633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Val662Ile
CA193972
NM_001324402.2:c.1984G>A