Allele Registry

Canonical Allele Identifier: PA2826658598

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015604

RCV000057405

ClinVar Variation:

14510

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Ser143Phe	CA018089 NM_001282625.2:c.428C>T