Allele Registry

Canonical Allele Identifier: PA2580181803

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002337803

RCV003108026

ClinVar Variation:

1743088

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln94Glu	CA346730594 NM_001258281.1:c.280C>G