Canonical Allele Identifier: PA2826660287
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 155896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Met348Ile
CA016471
NM_001282626.2:c.1044G>T
CA342820261
NM_001282626.2:c.1044G>A
CA342820262
NM_001282626.2:c.1044G>C