Canonical Allele Identifier: PA658662470
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 449753
ClinVar RCV Id: RCV000520158 RCV003403232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Met634Val
CA308420013
NM_181882.3:c.1900A>G