Canonical Allele Identifier: PA2826659522
Gene: LMNA HGNC NCBI
ClinVar RCV:
RCV001313361
ClinVar Variation:
1014606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg11Leu
CA342806869
NM_001282626.2:c.32G>T