Canonical Allele Identifier: PA218268
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Leu140Pro
CA018070
NM_170708.4:c.419T>C