Canonical Allele Identifier: PA2828780971
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 2633757
ClinVar RCV Id: RCV003408607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365406.2:p.Leu412Phe
CA329217086
NM_001378477.3:c.1234C>T