Allele Registry

Canonical Allele Identifier: PA2826463740

Gene: MSH2 HGNC NCBI

ClinVar Allele:

96016

ClinVar RCV:

RCV000574719

RCV000629732

RCV003997140

ClinVar Variation:

90541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn295Ser	CA017221 NM_001258281.1:c.884A>G