Allele Registry

Canonical Allele Identifier: PA2826463651

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000220354

RCV000232111

RCV000236110

RCV000662429

RCV003997950

ClinVar Variation:

232192

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu275Val	CA026646 NM_001258281.1:c.823C>G