Canonical Allele Identifier: PA218273
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Ser143Pro
CA018081
NM_170708.4:c.427T>C