Canonical Allele Identifier: PA2499284602
Gene: P3H2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016653
ClinVar RCV Id: RCV001315688
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060662.2:p.Ala193Val
CA2753304
NM_018192.4:c.578C>T