Canonical Allele Identifier: PA344695
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ala146Thr
CA018101
NM_170707.4:c.436G>A