Canonical Allele Identifier: PA2829298979
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004149418
ClinVar Variation:
2307265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387226.1:p.Ile785Phe
CA2392893
NM_001400297.1:c.2353A>T