Canonical Allele Identifier: PA299387
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182590
ClinVar RCV Id: RCV000160627 RCV000196535 RCV000491536 RCV000662661 RCV002265637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala256Thr
CA022219
NM_000251.3:c.766G>A