Canonical Allele Identifier: PA658662561
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 476971
ClinVar RCV Id: RCV000534630 RCV000790183
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Arg1380Cys
CA9443682
NM_181882.3:c.4138C>T