Canonical Allele Identifier: PA2580173109
Gene: NT5C1B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186016.1:p.Met337Ile
CA1541928
NM_001199087.2:c.1011G>T
CA1541929
NM_001199087.2:c.1011G>C
CA1541930
NM_001199087.2:c.1011G>A