Canonical Allele Identifier: PA2826660286
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66760
ClinVar RCV Id: RCV000057216 RCV001049424 RCV003996494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu347Lys
CA016456
NM_001282626.2:c.1039G>A