Canonical Allele Identifier: PA103581
Gene: NOP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 4279
ClinVar RCV Id: RCV000004500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061118.1:p.Arg34Trp
CA020161
NM_018648.4:c.100C>T