Canonical Allele Identifier: PA2828780937
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 99829
ClinVar RCV Id: RCV000086262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365406.2:p.Gly365Val
CA227938
NM_001378477.3:c.1094G>T