Canonical Allele Identifier: PA658807281
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 543498
ClinVar RCV Id: RCV000654272 RCV001173775 RCV002305523 RCV002325319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Val377Leu
CA9444320
NM_181882.3:c.1129G>T
CA405899021
NM_181882.3:c.1129G>C