Canonical Allele Identifier: PA1139709952
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 858698
ClinVar RCV Id: RCV001064629 RCV002402450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002519.2:p.Arg51Leu
CA7828353
NM_002528.7:c.152G>T