Canonical Allele Identifier: PA2826323717
Gene: P3H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 837722
ClinVar RCV Id: RCV001039117
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230175.1:p.Gly476Ser
CA801850
NM_001243246.2:c.1426G>A