Allele Registry

Canonical Allele Identifier: PA2826463078

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000526049

RCV000579804

RCV001584241

RCV004003753

ClinVar Variation:

455601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu139Gln	CA46678574 NM_001258281.1:c.415G>C