Canonical Allele Identifier: PA294578
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 155896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Met348Ile
CA016471
NM_170708.4:c.1044G>T
CA342820261
NM_170708.4:c.1044G>A
CA342820262
NM_170708.4:c.1044G>C