Canonical Allele Identifier: PA2826983724
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1777019
ClinVar RCV Id: RCV002394922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Val47Leu
CA394298004
NM_001318193.2:c.139G>T
CA394298006
NM_001318193.2:c.139G>C