Canonical Allele Identifier: PA2825929307
Gene: P3H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 837722
ClinVar RCV Id: RCV001039117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139761.1:p.Gly476Ser
CA801850
NM_001146289.2:c.1426G>A