Allele Registry

Canonical Allele Identifier: PA2826463165

Gene: MSH2 HGNC NCBI

ClinVar Allele:

518285

ClinVar RCV:

RCV000629696

ClinVar Variation:

525603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala164Val	CA346731902 NM_001258281.1:c.491C>T