Canonical Allele Identifier: PA355794
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 220724
ClinVar RCV Id: RCV000576841 RCV000762017 RCV001173957 RCV001795335 RCV001084142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Ala406Thr
CA349607
NM_181882.3:c.1216G>A