Canonical Allele Identifier: PA1139756850
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 959791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Thr394Ile
CA049322
NM_170708.4:c.1181C>T