Canonical Allele Identifier: PA2830008168
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 99829
ClinVar RCV Id: RCV000086262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_072089.2:p.Gly365Val
CA227938
NM_022567.3:c.1094G>T