Canonical Allele Identifier: PA2829408193
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3222668
ClinVar RCV Id: RCV004516052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002519.2:p.Asp99Val
CA394295549
NM_002528.7:c.296A>T