Canonical Allele Identifier: PA2826443764
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_001244303.1:p.Thr376Asn
CA342822741
NM_001257374.3:c.1127C>A