Canonical Allele Identifier: PA2826983888
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728057
ClinVar RCV Id: RCV002320689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Lys97Glu
CA394295617
NM_001318193.2:c.289A>G