Canonical Allele Identifier: PA2826657882
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2773542
ClinVar RCV Id: RCV003532559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Thr313Ser
CA342820910
NM_001282624.2:c.937A>T
CA342820917
NM_001282624.2:c.938C>G