Allele Registry

Canonical Allele Identifier: PA658812853

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000626229

RCV003581701

ClinVar Variation:

523026

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Pro20Leu	CA342807133 NM_170708.4:c.59C>T