Canonical Allele Identifier: PA2826443004
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66924
ClinVar Variation Id: 285122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Gly120Arg
CA018465
NM_001257374.3:c.358G>C
CA10605004
NM_001257374.3:c.358G>A