Canonical Allele Identifier: PA261942
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Leu369Pro
CA016599
NM_170707.4:c.1106T>C