Allele Registry

Canonical Allele Identifier: PA2826465331

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000492043

ClinVar Variation:

428504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile681del	CA645369197 NM_001258281.1:c.2037_2039del