Allele Registry

Canonical Allele Identifier: PA2826658980

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001324030

ClinVar Variation:

1023912

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Ser326Ala	CA342820087 NM_001282625.2:c.976T>G