Canonical Allele Identifier: PA645374503
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 380125
ClinVar RCV Id: RCV000687713 RCV001720038 RCV002429375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Val832Leu
CA9444045
NM_181882.3:c.2494G>C
CA405896167
NM_181882.3:c.2494G>T