Allele Registry

Canonical Allele Identifier: PA2826659652

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015600

RCV000057349

ClinVar Variation:

14506

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Ala57Pro	CA017669 NM_001282626.2:c.169G>C