Canonical Allele Identifier: PA2829648985
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

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