Allele Registry

Canonical Allele Identifier: PA658672320

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 455481

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys423Glu	CA027338 NM_000251.3:c.1267A>G