Canonical Allele Identifier: PA2826235795
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004213563
ClinVar Variation:
2377248
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186091.1:p.Ile825Thr
CA2392832
NM_001199162.2:c.2474T>C