Canonical Allele Identifier: PA658662586
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 476975
ClinVar RCV Id: RCV000526039 RCV001173943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Thr1445Ala
CA9443637
NM_181882.3:c.4333A>G