Allele Registry

Canonical Allele Identifier: PA2826463884

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001295164

ClinVar Variation:

999199

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln329Glu	CA346733845 NM_001258281.1:c.985C>G