Canonical Allele Identifier: PA2826660215
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1202871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu313Pro
CA342819726
NM_001282626.2:c.938T>C