Canonical Allele Identifier: PA2580405030
Gene: NOP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2150118
ClinVar RCV Id: RCV003067407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061118.1:p.Pro62Leu
CA268645224
NM_018648.4:c.185C>T