Allele Registry

Canonical Allele Identifier: PA916013554

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015604

RCV000057405

ClinVar Variation:

14510

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ser62Phe	CA018089 NM_001282624.2:c.185C>T