Canonical Allele Identifier: PA2826657514
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66924
ClinVar Variation Id: 285122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Gly151Arg
CA018465
NM_001282624.2:c.451G>C
CA10605004
NM_001282624.2:c.451G>A