Canonical Allele Identifier: PA2826443868
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14522
ClinVar RCV Id: RCV000015619 RCV000057331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Ala417Thr
CA017528
NM_001257374.3:c.1249G>A