Canonical Allele Identifier: PA124096
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Ala529Thr
CA017528
NM_170708.4:c.1585G>A