Allele Registry

Canonical Allele Identifier: PA2826657733

Gene: LMNA HGNC NCBI

ClinVar Allele:

77860

ClinVar RCV:

RCV000057496

RCV003581578

ClinVar Variation:

66963

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg250Pro	CA018942 NM_001282624.2:c.749G>C