Canonical Allele Identifier: PA916013532
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg52Leu
CA018044
NM_001282624.2:c.155G>T