Canonical Allele Identifier: PA218455
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66933
ClinVar RCV Id: RCV000057455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Tyr259His
CA018600
NM_005572.4:c.775T>C