Allele Registry

Canonical Allele Identifier: PA2826464632

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000220254

RCV000230549

RCV000663329

RCV001358260

RCV001800541

RCV001818514

ClinVar Variation:

229675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn517Ile	CA10577984 NM_001258281.1:c.1550A>T