Allele Registry

Canonical Allele Identifier: PA645474366

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000222532

RCV000236848

RCV000473755

RCV000663243

RCV003997770

ClinVar Variation:

229775

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu489Lys	CA10577978 NM_000251.3:c.1465G>A