Canonical Allele Identifier: PA217967
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Asp461Tyr
CA017154
NM_170708.4:c.1381G>T