Canonical Allele Identifier: PA2826659510
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1478493
ClinVar RCV Id: RCV002019020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg7Trp
CA342805997
NM_001282626.2:c.19C>T