Canonical Allele Identifier: PA916013561
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48067
ClinVar RCV Id: RCV000041350 RCV000057407 RCV001265661 RCV001852841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Thr69Pro
CA018114
NM_001282624.2:c.205A>C