Canonical Allele Identifier: PA2826659771
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1412782
ClinVar RCV Id: RCV001925536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu105Asp
CA342808753
NM_001282626.2:c.315G>C
CA342808754
NM_001282626.2:c.315G>T