Canonical Allele Identifier: PA658662449
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 476949
ClinVar RCV Id: RCV000539162 RCV001136190 RCV001565702 RCV002384261 RCV003915651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Glu457Lys
CA9444276
NM_181882.3:c.1369G>A