Canonical Allele Identifier: PA218323
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg189Trp
CA014940
NM_005572.4:c.565C>T