Allele Registry

Canonical Allele Identifier: PA2826463595

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000572560

RCV000629913

RCV000708829

RCV002483525

RCV003320694

ClinVar Variation:

480911

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn265Ser	CA042047 NM_001258281.1:c.794A>G