Canonical Allele Identifier: PA916071000
Gene: JPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 451220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787109.2:p.Thr76Ala
CA9868910
NM_175913.4:c.226A>G