Canonical Allele Identifier: PA2826658180
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_001269553.1:p.Arg460Ser
CA017601
NM_001282624.2:c.1378C>A