Allele Registry

Canonical Allele Identifier: PA2826464737

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160636

RCV000212610

RCV000462601

RCV000986680

ClinVar Variation:

182596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val539Ile	CA019367 NM_001258281.1:c.1615G>A