Canonical Allele Identifier: PA2826442941
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 65764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Leu103Pro
CA018372
NM_001257374.3:c.308T>C