Canonical Allele Identifier: PA916077730
Gene: USB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 496747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078874.2:p.His208Arg
CA396130121
NM_024598.4:c.623A>G