Canonical Allele Identifier: PA2826660105
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2900234
ClinVar RCV Id: RCV003745055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Lys261Glu
CA342817394
NM_001282626.2:c.781A>G