Canonical Allele Identifier: PA2826658464
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Glu84Asp
CA017807
NM_001282625.2:c.252G>C
CA342808461
NM_001282625.2:c.252G>T