Canonical Allele Identifier: PA915966609
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663122
ClinVar RCV Id: RCV000820927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro27Ala
CA346728680
NM_000251.3:c.79C>G