Canonical Allele Identifier: PA2828780948
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 1915373
ClinVar RCV Id: RCV002612978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365406.2:p.Glu385Asp
CA329217083
NM_001378477.3:c.1155G>C
CA412992909
NM_001378477.3:c.1155G>T