Canonical Allele Identifier: PA2826658109
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1332025
ClinVar RCV Id: RCV001804541 RCV001885271 RCV004009096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Pro428Ser
CA050569
NM_001282624.2:c.1282C>T