Canonical Allele Identifier: PA2829603411
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 502071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg298Pro
CA342817795
NM_005572.4:c.893G>C