Canonical Allele Identifier: PA2829182125
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004213563
ClinVar Variation:
2377248
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376536.1:p.Ile721Thr
CA2392832
NM_001389607.1:c.2162T>C