Canonical Allele Identifier: PA192569
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185668
ClinVar RCV Id: RCV000165126 RCV000464538 RCV001762374 RCV002498818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly25Cys
CA022143
NM_000251.3:c.73G>T