Canonical Allele Identifier: PA2829298426
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004213563
ClinVar Variation:
2377248
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387217.1:p.Ile837Thr
CA2392832
NM_001400288.1:c.2510T>C