Canonical Allele Identifier: PA2826983741
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2132471
ClinVar RCV Id: RCV003063807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305122.2:p.Lys52Asn
CA394297946
NM_001318193.2:c.156A>C
CA394297948
NM_001318193.2:c.156A>T