Canonical Allele Identifier: PA658803881
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525607
ClinVar RCV Id: RCV000629704 RCV000777452 RCV002233918 RCV004002771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr234Ala
CA346731985
NM_000251.3:c.700A>G