Canonical Allele Identifier: PA1139693538
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 926737
ClinVar RCV Id: RCV001189543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ile47Thr
CA053305
NM_001282624.2:c.140T>C