Canonical Allele Identifier: PA2826660035
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66925
ClinVar RCV Id: RCV000057445 RCV000201054 RCV001052813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Gly232Glu
CA018472
NM_001282626.2:c.695G>A