Canonical Allele Identifier: PA2826983777
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 641498
ClinVar RCV Id: RCV000794751 RCV002422698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Ser65Asn
CA7828342
NM_001318193.2:c.194G>A