Canonical Allele Identifier: PA2826660387
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2091332
ClinVar RCV Id: RCV003007932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu387Gln
CA342820759
NM_001282626.2:c.1160T>A