Canonical Allele Identifier: PA2579916665
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230812
ClinVar RCV Id: RCV004522926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro472Thr
CA346726781
NM_000251.3:c.1414C>A