Canonical Allele Identifier: PA2829602711
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_005563.1:p.Arg7Trp
CA342805997
NM_005572.4:c.19C>T