Allele Registry

Canonical Allele Identifier: PA2826657704

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057491

RCV000852590

RCV001182567

RCV001303998

RCV002371900

ClinVar Variation:

66961

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ala237Thr	CA018883 NM_001282624.2:c.709G>A