Canonical Allele Identifier: PA2825779865
Gene: P3H2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719103
ClinVar RCV Id: RCV002301863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127890.1:p.Arg11Thr
CA355759807
NM_001134418.2:c.32G>C