Canonical Allele Identifier: PA2827587631
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004213563
ClinVar Variation:
2377248
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338031.1:p.Ile721Thr
CA2392832
NM_001351102.2:c.2162T>C