Canonical Allele Identifier: PA116882
Gene: NT5C3A HGNC NCBI

Linked Data

ClinVar Variation Id: 4479
ClinVar RCV Id: RCV000004736 RCV003555917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057573.2:p.Asp98Val
CA116881
NM_016489.14:c.293A>T