Allele Registry

Canonical Allele Identifier: PA916057648

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001805960

RCV003117668

ClinVar Variation:

806245

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Gly608Cys	CA342827089 NM_170707.4:c.1822G>T