Canonical Allele Identifier: PA2826442749
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Ala34Thr
CA018101
NM_001257374.3:c.100G>A