Canonical Allele Identifier: PA2573165045
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494650
ClinVar RCV Id: RCV001989505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr225Ala
CA346731798
NM_000251.3:c.673A>G