Canonical Allele Identifier: PA166376
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141769
ClinVar RCV Id: RCV000130409 RCV000168465 RCV000509191 RCV000487305 RCV003998056 RCV004532559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val722Ile
CA020155
NM_000251.3:c.2164G>A