Canonical Allele Identifier: PA2826660698
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66859
ClinVar RCV Id: RCV000057341 RCV000823221 RCV004017361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg541Ser
CA017601
NM_001282626.2:c.1621C>A