Canonical Allele Identifier: PA2826062940
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 326
ClinVar RCV Id: RCV000000354 RCV000183674 RCV000208290 RCV000234084 RCV000246924 RCV000491470 RCV001170736 RCV003147270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Tyr588Cys
CA142143
NM_001172309.2:c.1763A>G