Canonical Allele Identifier: PA2828780963
Gene: NYX HGNC NCBI

Linked Data

ClinVar Variation Id: 1010626
ClinVar RCV Id: RCV001308282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365406.2:p.Ser406Arg
CA412993142
NM_001378477.3:c.1216A>C
CA412993152
NM_001378477.3:c.1218C>A
CA412993154
NM_001378477.3:c.1218C>G