Allele Registry

Canonical Allele Identifier: PA2826660778

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057356

ClinVar Variation:

66865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Cys588Arg	CA020344 NM_001282626.2:c.1762T>C