Canonical Allele Identifier: PA2826660027
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 180115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ile229Thr
CA018453
NM_001282626.2:c.686T>C