Canonical Allele Identifier: PA916013567
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 222692
ClinVar RCV Id: RCV000208276 RCV000536399 RCV000611547 RCV002327072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Thr69Ala
CA088193
NM_001282624.2:c.205A>G