Canonical Allele Identifier: PA103353
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg190Trp
CA018245
NM_170707.4:c.568C>T