Allele Registry

Canonical Allele Identifier: PA1139682242

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.7731212119

ClinVar RCV:

RCV001064476

RCV002429713

ClinVar Variation:

858581

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln879Lys	CA037172 NM_000251.3:c.2635C>A