Canonical Allele Identifier: PA2826659944
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg190Trp
CA018245
NM_001282626.2:c.568C>T