Allele Registry

Canonical Allele Identifier: PA2826442753

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001307001

RCV004005039

ClinVar Variation:

1009498

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ala35Thr	CA053436 NM_001257374.3:c.103G>A