Allele Registry

Canonical Allele Identifier: PA2826465482

Gene: MSH2 HGNC NCBI

ClinVar Allele:

181985

ClinVar RCV:

RCV000165012

RCV000196615

RCV000522265

RCV000587565

RCV003462160

RCV003995381

ClinVar Variation:

185569

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.His719Pro	CA020494 NM_001258281.1:c.2156A>C