Canonical Allele Identifier: PA916059515
Gene: UTP14C HGNC NCBI

Linked Data

ClinVar Variation Id: 312420
ClinVar RCV Id: RCV000294432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067677.4:p.Ser28Asn
CA10639716
NM_021645.6:c.83G>A