Canonical Allele Identifier: PA2826983720
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1309727
ClinVar RCV Id: RCV001756795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Pro46Ser
CA394298024
NM_001318193.2:c.136C>T