Allele Registry

Canonical Allele Identifier: PA2579911440

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002337803

RCV003108026

ClinVar Variation:

1743088

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln160Glu	CA346730594 NM_000251.3:c.478C>G