Canonical Allele Identifier: PA123988
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14479
ClinVar RCV Id: RCV000015567 RCV000015566 RCV000057359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg60Gly
CA017722
NM_170708.4:c.178C>G