Canonical Allele Identifier: PA2829648985
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_006668.1:p.Met982Leu
CA2392644
NM_006677.3:c.2944A>T
CA352735964
NM_006677.3:c.2944A>C