Canonical Allele Identifier: PA2826444096
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 570722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Ser513Cys
CA051489
NM_001257374.3:c.1537A>T