Allele Registry

Canonical Allele Identifier: PA2826464821

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000780453

RCV002413352

RCV003449268

ClinVar Variation:

427606

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro556Gln	CA346728465 NM_001258281.1:c.1667C>A