Canonical Allele Identifier: PA915954682
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663240
ClinVar RCV Id: RCV000821083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala831Pro
CA346730641
NM_000251.3:c.2491G>C