Allele Registry

Canonical Allele Identifier: PA2826628899

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115421

RCV000196523

RCV000212688

RCV000656901

RCV001139791

RCV001355140

RCV003467041

RCV003997251

ClinVar Variation:

127591

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Val1123Glu	CA014183 NM_001281492.2:c.3368T>A