Canonical Allele Identifier: PA2829182234
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004263351
ClinVar Variation:
2468045
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376537.1:p.Arg1214Trp
CA2392475
NM_001389608.1:c.3640C>T