Canonical Allele Identifier: PA2742009806
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 2564020
ClinVar RCV Id: RCV003306349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Ile10Ser
CA340884872
NM_144573.4:c.29T>G