Canonical Allele Identifier: PA2826658609
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 430306
ClinVar RCV Id: RCV000493099 RCV001060974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ala147Pro
CA342815415
NM_001282625.2:c.439G>C