Canonical Allele Identifier: PA915998888
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 647438
ClinVar RCV Id: RCV000801950 RCV003467387 RCV002256518 RCV003321744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002519.2:p.Tyr111Cys
CA7828322
NM_002528.7:c.332A>G