Allele Registry

Canonical Allele Identifier: PA2826464723

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000205416

RCV000221565

RCV000235312

RCV000663070

RCV001356036

RCV003997576

ClinVar Variation:

219668

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu536Val	CA031475 NM_001258281.1:c.1606C>G