Allele Registry

Canonical Allele Identifier: PA218169

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057373

ClinVar Variation:

66876

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Arg614Ser	CA015174 NM_170708.4:c.1840C>A