Canonical Allele Identifier: PA916079013
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 659455
ClinVar RCV Id: RCV000816467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.His741Tyr
CA405896736
NM_181882.3:c.2221C>T