Canonical Allele Identifier: PA2826983929
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823878
ClinVar RCV Id: RCV001020505
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.His109Gln
CA394295217
NM_001318193.2:c.327C>G
CA394295219
NM_001318193.2:c.327C>A