Canonical Allele Identifier: PA2826443855
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg415Pro
CA017498
NM_001257374.3:c.1244G>C