Allele Registry

Canonical Allele Identifier: PA2826464164

Gene: MSH2 HGNC NCBI

ClinVar Allele:

472926

ClinVar RCV:

RCV000567509

RCV000685208

RCV000759100

RCV003459384

RCV004001116

ClinVar Variation:

485825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Met394Thr	CA346724826 NM_001258281.1:c.1181T>C