Allele Registry

Canonical Allele Identifier: PA2826658453

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000237077

RCV001351546

ClinVar Variation:

246580

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Tyr81Cys	CA10584114 NM_001282625.2:c.242A>G