Allele Registry

Canonical Allele Identifier: PA2826444163

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057373

ClinVar Variation:

66876

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg532Ser	CA015174 NM_001257374.3:c.1594C>A