Canonical Allele Identifier: PA2826983937
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 864092
ClinVar RCV Id: RCV001071197 RCV002451310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Asp112Glu
CA394295131
NM_001318193.2:c.336C>G
CA394295133
NM_001318193.2:c.336C>A