Canonical Allele Identifier: PA645374654
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 246041
ClinVar RCV Id: RCV000236345 RCV000542374 RCV001172769 RCV001824704 RCV001358804 RCV002327160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Ser1407Ala
CA9443662
NM_181882.3:c.4219T>G