Canonical Allele Identifier: PA2579920476
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785830
ClinVar RCV Id: RCV002424142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala700Thr
CA346729229
NM_000251.3:c.2098G>A