Canonical Allele Identifier: PA2830406926
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 2116697
ClinVar RCV Id: RCV003024848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Glu773Gln
CA405896549
NM_181882.3:c.2317G>C