Canonical Allele Identifier: PA2826444032
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Asp484Asn
CA051326
NM_001257374.3:c.1450G>A