Canonical Allele Identifier: PA160879
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41648
ClinVar RCV Id: RCV000034556 RCV000121564 RCV000129519 RCV001080801 RCV001093691 RCV001030484 RCV001356651 RCV001787035 RCV004534720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu809Lys
CA020577
NM_000251.3:c.2425G>A