Allele Registry

Canonical Allele Identifier: PA658738986

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.1760780193

ClinVar RCV:

RCV000579590

RCV001240812

RCV001574074

RCV004001257

ClinVar Variation:

489929

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Thr677Ala	CA346729112 NM_000251.3:c.2029A>G