Canonical Allele Identifier: PA916013541
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66898
ClinVar RCV Id: RCV000057402 RCV001854176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu59Pro
CA018070
NM_001282624.2:c.176T>C