Allele Registry

Canonical Allele Identifier: PA2826658079

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000594075

RCV001867919

ClinVar Variation:

497324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Gln412Pro	CA342822801 NM_001282624.2:c.1235A>C