Canonical Allele Identifier: PA2741842295
Gene: NT5C1B HGNC NCBI
ClinVar RCV:
RCV004353338
ClinVar Variation:
2607709
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186016.1:p.Ser312Gly
CA1541972
NM_001199087.2:c.934A>G