Allele Registry

Canonical Allele Identifier: PA2826463833

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000490918

RCV000704685

RCV001264478

RCV004003471

RCV004527600

ClinVar Variation:

428531

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg317Gln	CA027092 NM_001258281.1:c.950G>A