Allele Registry

Canonical Allele Identifier: PA124079

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015615

RCV000057443

ClinVar Variation:

14518

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Asp230Asn	CA018460 NM_170708.4:c.688G>A