Canonical Allele Identifier: PA2826659532
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1350707
ClinVar RCV Id: RCV002042071 RCV002489934 RCV004009185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ala16Asp
CA053561
NM_001282626.2:c.47C>A