Canonical Allele Identifier: PA2830328090
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2749065
ClinVar RCV Id: RCV003582812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Asp511Glu
CA342823198
NM_170707.4:c.1533C>A
CA342823201
NM_170707.4:c.1533C>G