Allele Registry

Canonical Allele Identifier: PA2826462932

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000204442

RCV000214137

RCV000759837

RCV002485345

RCV003315420

RCV003320603

RCV003997618

ClinVar Variation:

220157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln104Glu	CA039073 NM_001258281.1:c.310C>G