Canonical Allele Identifier: PA891857182
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 570722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ser625Cys
CA051489
NM_170707.4:c.1873A>T