Canonical Allele Identifier: PA2826660536
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66811
ClinVar RCV Id: RCV000057277 RCV000465598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asn456Asp
CA017074
NM_001282626.2:c.1366A>G