Canonical Allele Identifier: PA2826659311
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1522462
ClinVar RCV Id: RCV002034441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asp475Gly
CA342822584
NM_001282625.2:c.1424A>G