Canonical Allele Identifier: PA2826659412
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ala529Thr
CA017528
NM_001282625.2:c.1585G>A