Allele Registry

Canonical Allele Identifier: PA916013582

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000041352

RCV000057410

ClinVar Variation:

48068

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Leu81Pro	CA018144 NM_001282624.2:c.242T>C