Allele Registry

Canonical Allele Identifier: PA645473100

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000220354

RCV000232111

RCV000236110

RCV000662429

RCV003997950

ClinVar Variation:

232192

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu341Val	CA026646 NM_000251.3:c.1021C>G