Canonical Allele Identifier: PA2826660368
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu380Ser
CA016670
NM_001282626.2:c.1139T>C