Canonical Allele Identifier: PA2826657523
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 180404
ClinVar RCV Id: RCV000157292 RCV002362839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Phe156Ser
CA018485
NM_001282624.2:c.467T>C