Canonical Allele Identifier: PA645491841
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 298090
ClinVar RCV Id: RCV000344842 RCV000403905 RCV001850571 RCV002411191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Ile631Thr
CA919000
NM_144573.4:c.1892T>C