Canonical Allele Identifier: PA2826660593
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1715530
ClinVar RCV Id: RCV002301304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr488Asn
CA342822741
NM_001282626.2:c.1463C>A