Canonical Allele Identifier: PA2826659341
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 497324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Gln493Pro
CA342822801
NM_001282625.2:c.1478A>C