Allele Registry

Canonical Allele Identifier: PA2826462934

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001968134

ClinVar Variation:

1442232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln104Lys	CA346730695 NM_001258281.1:c.310C>A