Canonical Allele Identifier: PA154814
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 130053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Gly1132Arg
CA154812
NM_181882.3:c.3394G>A
CA405893929
NM_181882.3:c.3394G>C