Allele Registry

Canonical Allele Identifier: PA2826463043

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000204459

RCV000480096

RCV000772140

RCV003997653

ClinVar Variation:

220812

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys131Glu	CA348678 NM_001258281.1:c.391A>G