Canonical Allele Identifier: PA2827587475
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_001338029.1:p.Met1084Leu
CA2392644
NM_001351100.2:c.3250A>T
CA352735964
NM_001351100.2:c.3250A>C