Allele Registry

Canonical Allele Identifier: PA2826659537

Gene: LMNA HGNC NCBI

ClinVar Allele:

513494

ClinVar RCV:

RCV000626229

RCV003581701

ClinVar Variation:

523026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Pro20Leu	CA342807133 NM_001282626.2:c.59C>T