Canonical Allele Identifier: PA2826983901
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2691961
ClinVar RCV Id: RCV003494158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Pro101Leu
CA394295508
NM_001318193.2:c.302C>T