Canonical Allele Identifier: PA658662437
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 476979
ClinVar RCV Id: RCV000554182 RCV001546675 RCV002377182 RCV001131934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Arg240Gln
CA9444391
NM_181882.3:c.719G>A