Allele Registry

Canonical Allele Identifier: PA2826464269

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000222532

RCV000236848

RCV000473755

RCV000663243

RCV003997770

ClinVar Variation:

229775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu423Lys	CA10577978 NM_001258281.1:c.1267G>A