Canonical Allele Identifier: PA2826658267
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1256329
ClinVar RCV Id: RCV001663671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ala14Glu
CA342806964
NM_001282625.2:c.41C>A