Allele Registry

Canonical Allele Identifier: PA2826660236

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003319250

ClinVar Variation:

2505317

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Glu324del	CA2580612542 NM_001282626.2:c.972_974del