Canonical Allele Identifier: PA2827587787
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004149418
ClinVar Variation:
2307265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338033.1:p.Ile701Phe
CA2392893
NM_001351104.2:c.2101A>T