Canonical Allele Identifier: PA2826660329
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1717360
ClinVar RCV Id: RCV002297554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu363Gln
CA342820380
NM_001282626.2:c.1088T>A