Allele Registry

Canonical Allele Identifier: PA2826465377

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000464961

RCV000573097

RCV000583000

RCV000781562

RCV001788225

RCV003228932

RCV004000793

ClinVar Variation:

408544

491802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr690Ser	CA035142 NM_001258281.1:c.2069C>G CA46704862 NM_001258281.1:c.2068A>T