Canonical Allele Identifier: PA2826660236
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2505317
ClinVar RCV Id: RCV003319250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu324del
CA342820036
NM_001282626.2:c.970G>T
CA2580612542
NM_001282626.2:c.972_974del