Canonical Allele Identifier: PA104315
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ser295Pro
CA018804
NM_170707.4:c.883T>C