Canonical Allele Identifier: PA2826660403
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 959791
ClinVar RCV Id: RCV001233202 RCV004004848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr394Ile
CA049322
NM_001282626.2:c.1181C>T