Canonical Allele Identifier: PA2573283221
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 1499111
ClinVar RCV Id: RCV002010426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_072089.2:p.Thr391Ser
CA10389917
NM_022567.3:c.1171A>T