Canonical Allele Identifier: PA218289
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66900
ClinVar RCV Id: RCV000057408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Glu159Lys
CA018134
NM_170708.4:c.475G>A