Canonical Allele Identifier: PA2828504844
Gene: NT5C3A HGNC NCBI

Linked Data

ClinVar Variation Id: 4479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361265.1:p.Asp86Val
CA116881
NM_001374336.1:c.257A>T