Canonical Allele Identifier: PA2826657390
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2821715
ClinVar RCV Id: RCV003744194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Glu78Gln
CA342815561
NM_001282624.2:c.232G>C