Canonical Allele Identifier: PA2830327379
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 580670
ClinVar RCV Id: RCV000704281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ile373Met
CA342820516
NM_170707.4:c.1119C>G