Canonical Allele Identifier: PA2826658534
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1436689
ClinVar RCV Id: RCV001946419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Lys114Gln
CA342808876
NM_001282625.2:c.340A>C