Allele Registry

Canonical Allele Identifier: PA2826465507

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000132529

RCV000409026

RCV000540856

RCV001354926

RCV001650987

RCV001818334

ClinVar Variation:

143010

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn726Ser	CA020519 NM_001258281.1:c.2177A>G