Canonical Allele Identifier: PA2830101531
Gene: NT5C1B HGNC NCBI
ClinVar RCV:
RCV004198263
ClinVar Variation:
2358408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_150278.2:p.Met260Ile
CA1541928
NM_033253.4:c.780G>T
CA1541929
NM_033253.4:c.780G>C
CA1541930
NM_033253.4:c.780G>A