Canonical Allele Identifier: PA2826659517
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 864820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg8His
CA342806023
NM_001282626.2:c.23G>A