Canonical Allele Identifier: PA2826658173
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66858
ClinVar RCV Id: RCV000057340 RCV000192012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Met459Thr
CA017588
NM_001282624.2:c.1376T>C