Canonical Allele Identifier: PA217871
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66799
ClinVar RCV Id: RCV000057262 RCV001225020
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Ala43Thr
CA016942
NM_170708.4:c.127G>A