Allele Registry

Canonical Allele Identifier: PA104111

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015601

RCV000057403

ClinVar Variation:

14507

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Leu140Arg	CA018076 NM_170707.4:c.419T>G