Canonical Allele Identifier: PA2826659825
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 222691
ClinVar RCV Id: RCV000208154
ClinVar Variation Id: 476828
ClinVar RCV Id: RCV000543428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp126Glu
CA351809
NM_001282626.2:c.378C>G
CA342815084
NM_001282626.2:c.378C>A