Allele Registry

Canonical Allele Identifier: PA2826626485

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001322251

RCV001806119

ClinVar Variation:

1022358

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu487Ile	CA068196 NM_001281492.2:c.1459C>A