Allele Registry

Canonical Allele Identifier: PA331416

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.921304924

ClinVar Allele:

96298

ClinVar RCV:

RCV000076325

ClinVar Variation:

90823

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Pro652His	CA019605 NM_000251.3:c.1955C>A