Allele Registry

Canonical Allele Identifier: PA913193536

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000774957

ClinVar Variation:

630048

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln861Glu	CA346730999 NM_000251.3:c.2581C>G