Allele Registry

Canonical Allele Identifier: PA2826463882

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002335486

ClinVar Variation:

1742736

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln329Lys	CA346733843 NM_001258281.1:c.985C>A