Canonical Allele Identifier: PA645374520
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 245910
ClinVar RCV Id: RCV000474498 RCV000766571 RCV001131681 RCV001172762 RCV001283504 RCV001814975 RCV002321902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Lys1062Asn
CA9443909
NM_181882.3:c.3186G>T
CA405894769
NM_181882.3:c.3186G>C