Canonical Allele Identifier: PA2826659608
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66799
ClinVar RCV Id: RCV000057262 RCV001225020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ala43Thr
CA016942
NM_001282626.2:c.127G>A