Allele Registry

Canonical Allele Identifier: PA658671928

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000544343

RCV001764526

RCV002289719

RCV004023722

ClinVar Variation:

455615

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu270Val	CA040694 NM_000251.3:c.808C>G