Canonical Allele Identifier: PA124038
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg527His
CA014822
NM_170708.4:c.1580G>A