Canonical Allele Identifier: PA2826659531
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2843506
ClinVar RCV Id: RCV003744450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ala16Val
CA342807040
NM_001282626.2:c.47C>T