Allele Registry

Canonical Allele Identifier: PA2827597397

Gene: NT5C2 HGNC NCBI

ClinVar RCV:

RCV000441591

RCV001511967

ClinVar Variation:

380851

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338099.1:p.Thr3Ala	CA5671217 NM_001351170.2:c.7A>G