Allele Registry

Canonical Allele Identifier: PA2826462981

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001207699

ClinVar Variation:

938476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln117Glu	CA346730871 NM_001258281.1:c.349C>G