Canonical Allele Identifier: PA2826659492
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200967
ClinVar RCV Id: RCV000726056 RCV001182259 RCV001394831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg572Cys
CA017711
NM_001282625.2:c.1714C>T