Allele Registry

Canonical Allele Identifier: PA2826464227

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000485109

RCV000572164

RCV000698504

RCV003470555

RCV004003319

ClinVar Variation:

420083

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu412Phe	CA16617579 NM_001258281.1:c.1234C>T