Allele Registry

Canonical Allele Identifier: PA2826659656

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015627

RCV000057357

ClinVar Variation:

18457

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Leu59Arg	CA017717 NM_001282626.2:c.176T>G