Canonical Allele Identifier: PA124003
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg527Cys
CA017487
NM_005572.4:c.1579C>T