Allele Registry

Canonical Allele Identifier: PA2826464719

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000205243

RCV000567614

RCV000765669

RCV002469065

RCV003477681

ClinVar Variation:

219605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln535Arg	CA031443 NM_001258281.1:c.1604A>G