Allele Registry

Canonical Allele Identifier: PA2826465492

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002457714

ClinVar Variation:

1790186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr722Ser	CA346730014 NM_001258281.1:c.2164A>T CA346730020 NM_001258281.1:c.2165C>G