Allele Registry

Canonical Allele Identifier: PA915984272

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000568245

RCV000630061

RCV001584374

RCV004000906

ClinVar Variation:

480910

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala88Thr	CA038871 NM_001258281.1:c.262G>A