Allele Registry

Canonical Allele Identifier: PA2826464315

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000115502

RCV000222010

RCV000475133

RCV001527007

RCV003460819

RCV003997270

RCV004529930

ClinVar Variation:

127630

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asp436Gly	CA018475 NM_001258281.1:c.1307A>G