Canonical Allele Identifier: PA2826983712
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2880126
ClinVar RCV Id: RCV003713140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.His44Gln
CA394298042
NM_001318193.2:c.132C>G
CA394298044
NM_001318193.2:c.132C>A