Allele Registry

Canonical Allele Identifier: PA2826464137

Gene: MSH2 HGNC NCBI

ClinVar Allele:

392878

ClinVar RCV:

RCV000467391

RCV000491177

RCV001764410

RCV003463909

RCV004000792

ClinVar Variation:

408536

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile388Thr	CA16610869 NM_001258281.1:c.1163T>C