Allele Registry

Canonical Allele Identifier: PA2579923511

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.8533783091

ClinVar RCV:

RCV004014351

ClinVar Variation:

3074817

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln879His	CA346731321 NM_000251.3:c.2637A>C CA346731322 NM_000251.3:c.2637A>T