Canonical Allele Identifier: PA658672329
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483719
ClinVar RCV Id: RCV000570734 RCV002528137 RCV004001039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His428Asp
CA346724494
NM_000251.3:c.1282C>G