Allele Registry

Canonical Allele Identifier: PA2826463118

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000216132

RCV000541467

RCV003159097

RCV003997179

ClinVar Variation:

91171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile150Val	CA021692 NM_001258281.1:c.448A>G