Canonical Allele Identifier: PA2830019079
Gene: USB1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078874.2:p.Met116Arg
CA396129119
NM_024598.4:c.347T>G