Canonical Allele Identifier: PA2573164922
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1486126
ClinVar RCV Id: RCV002001252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe276Cys
CA346732795
NM_000251.3:c.827T>G