Canonical Allele Identifier: PA2499230002
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1042963
ClinVar RCV Id: RCV001347002 RCV003169693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala623Thr
CA346728468
NM_000251.3:c.1867G>A