Allele Registry

Canonical Allele Identifier: PA2826463058

Gene: MSH2 HGNC NCBI

ClinVar Allele:

96623

ClinVar RCV:

RCV000076652

RCV000811653

RCV002354270

ClinVar Variation:

91148

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val134Asp	CA021536 NM_001258281.1:c.401T>A