Canonical Allele Identifier: PA2829602980
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2098083
ClinVar RCV Id: RCV003030763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Leu106Pro
CA342808766
NM_005572.4:c.317T>C