Canonical Allele Identifier: PA2499302258
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 1061093
ClinVar RCV Id: RCV001370611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Pro730Ser
CA405896809
NM_181882.3:c.2188C>T