Canonical Allele Identifier: PA2573165068
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384112
ClinVar RCV Id: RCV001895755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu590Gly
CA346728268
NM_000251.3:c.1769A>G