Allele Registry

Canonical Allele Identifier: PA217699

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057220

RCV003581571

ClinVar Variation:

66764

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Ala350Pro	CA016496 NM_005572.4:c.1048G>C