Canonical Allele Identifier: PA2825078893
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230851
ClinVar RCV Id: RCV004522965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe23del
CA2825001108
NM_000251.3:c.66_68del