Allele Registry

Canonical Allele Identifier: PA2826464684

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000163932

RCV000554840

RCV001267891

ClinVar Variation:

184645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu529Arg	CA019291 NM_001258281.1:c.1586T>G