Canonical Allele Identifier: PA103651
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg527Pro
CA017498
NM_170707.4:c.1580G>C