Canonical Allele Identifier: PA2573165199
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477123
ClinVar RCV Id: RCV001971429 RCV003493902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys843Gly
CA346730778
NM_000251.3:c.2527T>G