Canonical Allele Identifier: PA2826983872
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 647900
ClinVar RCV Id: RCV000802521 RCV001017892 RCV002268292 RCV002501079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Arg92His
CA7828331
NM_001318193.2:c.275G>A