Canonical Allele Identifier: PA2826659087
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1467968
ClinVar RCV Id: RCV001968762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Glu372Gly
CA342820499
NM_001282625.2:c.1115A>G