Canonical Allele Identifier: PA645374588
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 245824
ClinVar RCV Id: RCV000236523 RCV000764201 RCV000819134 RCV002347921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Gly1257Arg
CA9443791
NM_181882.3:c.3769G>A
CA405892273
NM_181882.3:c.3769G>C