Canonical Allele Identifier: PA2827587802
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2457594
ClinVar RCV Id: RCV004248729
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338033.1:p.Met986Leu
CA2392644
NM_001351104.2:c.2956A>T
CA352735964
NM_001351104.2:c.2956A>C