Canonical Allele Identifier: PA076794
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 222753
ClinVar RCV Id: RCV000208073 RCV000248087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Ile467Thr
CA076791
NM_144573.4:c.1400T>C