Allele Registry

Canonical Allele Identifier: PA2826657464

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015588

RCV000057433

ClinVar Variation:

66918

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Lys127del	CA018324 NM_001282624.2:c.381_383del