Allele Registry

Canonical Allele Identifier: PA2826443275

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003319250

ClinVar Variation:

2505317

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Glu212del	CA2580612542 NM_001257374.3:c.636_638del