Canonical Allele Identifier: PA2826657704
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66961
ClinVar RCV Id: RCV000057491 RCV000852590 RCV001182567 RCV001303998 RCV002371900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ala237Thr
CA018883
NM_001282624.2:c.709G>A