Canonical Allele Identifier: PA218386
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 65764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Leu215Pro
CA018372
NM_170708.4:c.644T>C