Canonical Allele Identifier: PA299327
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182566
ClinVar RCV Id: RCV000160594 RCV000539963 RCV001025106 RCV003998475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg21His
CA021613
NM_000251.3:c.62G>A