Canonical Allele Identifier: PA2826659739
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 849968
ClinVar RCV Id: RCV001054035 RCV001170450 RCV004031698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu92Val
CA342808563
NM_001282626.2:c.274C>G