Canonical Allele Identifier: PA218218
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Thr10Ile
CA017867
NM_170708.4:c.29C>T