Canonical Allele Identifier: PA2826658338
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66791
ClinVar RCV Id: RCV000057252 RCV000557302 RCV004545742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asn39Ser
CA016815
NM_001282625.2:c.116A>G