Canonical Allele Identifier: PA2829604031
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2749065
ClinVar RCV Id: RCV003582812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Asp511Glu
CA342823198
NM_005572.4:c.1533C>A
CA342823201
NM_005572.4:c.1533C>G