Canonical Allele Identifier: PA2828780925
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 2059548
ClinVar RCV Id: RCV002952858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365406.2:p.Met346Leu
CA10389900
NM_001378477.3:c.1036A>C
CA412992170
NM_001378477.3:c.1036A>T