Canonical Allele Identifier: PA2573164934
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482359
ClinVar RCV Id: RCV002002906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala306Gly
CA346732976
NM_000251.3:c.917C>G