Allele Registry

Canonical Allele Identifier: PA2826657772

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057220

RCV003581571

ClinVar Variation:

66764

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ala269Pro	CA016496 NM_001282624.2:c.805G>C