Allele Registry

Canonical Allele Identifier: PA2579910403

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001229724

ClinVar Variation:

956843

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu101Gln	CA346729628 NM_000251.3:c.301G>C