Canonical Allele Identifier: PA645502448
Gene: NOP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 235529
ClinVar RCV Id: RCV000224102 RCV000503008 RCV001084193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061118.1:p.Asp12His
CA7464815
NM_018648.4:c.34G>C