Canonical Allele Identifier: PA2742010785
Gene: NAXE HGNC NCBI

Linked Data

ClinVar Variation Id: 1802682
ClinVar RCV Id: RCV003232627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_658985.2:p.Cys158Ser
CA1162783
NM_144772.3:c.473G>C
CA342873717
NM_144772.3:c.472T>A