Allele Registry

Canonical Allele Identifier: PA2826657729

Gene: LMNA HGNC NCBI

ClinVar Allele:

1002177

ClinVar RCV:

RCV001317047

ClinVar Variation:

1017837

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Glu249Lys	CA342820135 NM_001282624.2:c.745G>A