Canonical Allele Identifier: PA2580291138
Gene: UVRAG HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003360.2:p.Thr212Ile
CA381978067
NM_003369.4:c.635C>T