Canonical Allele Identifier: PA645426020
Gene: P3H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 379444
ClinVar RCV Id: RCV000443398 RCV000532565 RCV001101548
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071751.3:p.Gly349Arg
CA801996
NM_022356.4:c.1045G>A
CA339958828
NM_022356.4:c.1045G>C