Allele Registry

Canonical Allele Identifier: PA2826444012

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057356

ClinVar Variation:

66865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Cys476Arg	CA020344 NM_001257374.3:c.1426T>C