Canonical Allele Identifier: PA658816635
Gene: NOP56 HGNC NCBI

Linked Data

ClinVar Variation Id: 523492
ClinVar RCV Id: RCV000626898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006383.2:p.Ser151Thr
CA408024295
NM_006392.4:c.452G>C