Canonical Allele Identifier: PA217819
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg388Cys
CA016798
NM_005572.4:c.1162C>T