Canonical Allele Identifier: PA2826443444
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg265Leu
CA016657
NM_001257374.3:c.794G>T