Canonical Allele Identifier: PA2826659501
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 921978
ClinVar RCV Id: RCV001181741 RCV003769991 RCV004006760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr3Asn
CA342805896
NM_001282626.2:c.8C>A