Allele Registry

Canonical Allele Identifier: PA095191

Gene: MSH2 HGNC NCBI

MaveDb:

Score 2.5348008718

ClinVar RCV:

RCV000076611

RCV001183049

ClinVar Variation:

91108

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val163Gly	CA021209 NM_000251.3:c.488T>G