Canonical Allele Identifier: PA2826659500
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1362553
ClinVar RCV Id: RCV001900220 RCV003130563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr3Ala
CA342805889
NM_001282626.2:c.7A>G