Canonical Allele Identifier: PA2826232521
Gene: NT5C1B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186015.1:p.Ile63Thr
CA1542188
NM_001199086.2:c.188T>C