Canonical Allele Identifier: PA2826444063
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Gly496Ser
CA015235
NM_001257374.3:c.1486G>A