Canonical Allele Identifier: PA645471204
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408530
ClinVar RCV Id: RCV000563687 RCV002230365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln61Glu
CA16610991
NM_000251.3:c.181C>G