Canonical Allele Identifier: PA645471205
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233513
ClinVar RCV Id: RCV000216596 RCV000537297 RCV001753678
ClinVar Variation Id: 483733
ClinVar RCV Id: RCV000571464 RCV000679297 RCV001858303 RCV004001042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln61His
CA031678
NM_000251.3:c.183G>C
CA031694
NM_000251.3:c.183G>T