Canonical Allele Identifier: PA2826062678
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 201925
ClinVar RCV Id: RCV000223852 RCV000535150 RCV000845501 RCV000619532 RCV000766517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Leu415Phe
CA335415
NM_001172309.2:c.1243C>T