Allele Registry

Canonical Allele Identifier: PA2826464820

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000256112

RCV000491622

RCV000506471

RCV000629692

RCV003454782

ClinVar Variation:

265573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro556Arg	CA10588344 NM_001258281.1:c.1667C>G