Canonical Allele Identifier: PA2573272929
Gene: P3H2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497607
ClinVar RCV Id: RCV002019474
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060662.2:p.Val176Leu
CA2753315
NM_018192.4:c.526G>C
CA355759920
NM_018192.4:c.526G>T