Canonical Allele Identifier: PA104355
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Thr528Arg
CA017510
NM_170707.4:c.1583C>G