Canonical Allele Identifier: PA2826983891
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948307
ClinVar RCV Id: RCV001219533 RCV002322061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Asp99Ala
CA276765608
NM_001318193.2:c.296A>C