Allele Registry

Canonical Allele Identifier: PA2826660796

Gene: LMNA HGNC NCBI

ClinVar Allele:

427656

ClinVar RCV:

RCV000503392

RCV000653834

RCV000992277

RCV001526033

RCV004003526

ClinVar Variation:

435774

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Asp596Asn	CA051326 NM_001282626.2:c.1786G>A