Canonical Allele Identifier: PA2826659587
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1422153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Gln36His
CA342807575
NM_001282626.2:c.108G>C
CA342807583
NM_001282626.2:c.108G>T