Allele Registry

Canonical Allele Identifier: PA2826658639

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000041352

RCV000057410

ClinVar Variation:

48068

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Leu162Pro	CA018144 NM_001282625.2:c.485T>C