Canonical Allele Identifier: PA916059513
Gene: UTP14C HGNC NCBI

Linked Data

ClinVar Variation Id: 312419
ClinVar RCV Id: RCV000384111
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067677.4:p.Leu21Phe
CA6990126
NM_021645.6:c.63G>T
CA388026885
NM_021645.6:c.63G>C