Canonical Allele Identifier: PA262001
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Tyr267His
CA018657
NM_170707.4:c.799T>C