Canonical Allele Identifier: PA645471838
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 433878
ClinVar RCV Id: RCV001355023 RCV001368191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly220Glu
CA346731709
NM_000251.3:c.659G>A