Canonical Allele Identifier: PA1139710187
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948042
ClinVar RCV Id: RCV001219220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002519.2:p.Trp79Cys
CA394297255
NM_002528.7:c.237G>T
CA394297262
NM_002528.7:c.237G>C