Canonical Allele Identifier: PA124079
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Asp230Asn
CA018460
NM_170708.4:c.688G>A