Allele Registry

Canonical Allele Identifier: PA915984146

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000492034

RCV000587688

RCV000629990

RCV000986650

RCV003998482

ClinVar Variation:

182577

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser63Cys	CA021106 NM_001258281.1:c.188C>G