Canonical Allele Identifier: PA2827254695
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 41624
ClinVar RCV Id: RCV000034529 RCV000121340 RCV000123120 RCV000163261 RCV000203290 RCV000431770 RCV000421063 RCV001507182 RCV002227927 RCV003891465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr562Ile
CA160417
NM_001324402.2:c.1685C>T