Canonical Allele Identifier: PA2826983905
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371438
ClinVar RCV Id: RCV001878999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Val102Gly
CA394295453
NM_001318193.2:c.305T>G