Canonical Allele Identifier: PA2826232631
Gene: NT5C1B HGNC NCBI
ClinVar RCV:
RCV004353338
ClinVar Variation:
2607709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186017.1:p.Ser297Gly
CA1541972
NM_001199088.2:c.889A>G