Canonical Allele Identifier: PA2830327900
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2567283
ClinVar RCV Id: RCV003311163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ser463Tyr
CA31014100
NM_170707.4:c.1388C>A