Canonical Allele Identifier: PA2826983936
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 662685
ClinVar RCV Id: RCV000820392 RCV002257986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Asp112Asn
CA276765589
NM_001318193.2:c.334G>A