Canonical Allele Identifier: PA645472955
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408558
ClinVar RCV Id: RCV000575104 RCV000457800 RCV000663211 RCV000852299 RCV001584155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala328Thr
CA16610859
NM_000251.3:c.982G>A