Canonical Allele Identifier: PA2826658177
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 29775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg460Gly
CA017607
NM_001282624.2:c.1378C>G