Allele Registry

Canonical Allele Identifier: PA2830330032

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001805960

RCV003117668

ClinVar Variation:

806245

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Gly578Cys	CA342827089 NM_170708.4:c.1732G>T