Canonical Allele Identifier: PA2826659999
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 65764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu215Pro
CA018372
NM_001282626.2:c.644T>C