Canonical Allele Identifier: PA218148
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg594His
CA015260
NM_170708.4:c.1781G>A