Allele Registry

Canonical Allele Identifier: PA2826463024

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002359701

ClinVar Variation:

1749593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln127Lys	CA346730972 NM_001258281.1:c.379C>A