Canonical Allele Identifier: PA2829408172
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3222665
ClinVar RCV Id: RCV004516049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002519.2:p.Lys75Gln
CA394297390
NM_002528.7:c.223A>C