Allele Registry

Canonical Allele Identifier: PA1139678094

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001038694

ClinVar Variation:

837376

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln377Glu	CA027045 NM_000251.3:c.1129C>G