Canonical Allele Identifier: PA1139710297
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 845369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002519.2:p.Thr107Pro
CA276765601
NM_002528.7:c.319A>C