Canonical Allele Identifier: PA248996
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 216835
ClinVar RCV Id: RCV000202796 RCV001086843 RCV001172771 RCV001509034 RCV001135981 RCV002453729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Pro1166Ser
CA248994
NM_181882.3:c.3496C>T