Canonical Allele Identifier: PA2573303427
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1360466
ClinVar RCV Id: RCV001904900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Asp648Gly
CA919010
NM_144573.4:c.1943A>G