Allele Registry

Canonical Allele Identifier: PA2826464491

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000479671

RCV000490983

RCV000524350

RCV003317077

RCV003466965

RCV003997151

ClinVar Variation:

90714

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly482Cys	CA018790 NM_001258281.1:c.1444G>T