Allele Registry

Canonical Allele Identifier: PA2826464390

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160592

RCV000218047

RCV000228006

RCV000708832

RCV002243830

RCV003467248

RCV003492653

ClinVar Variation:

182564

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg458His	CA018637 NM_001258281.1:c.1373G>A