Canonical Allele Identifier: PA1139748016
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 917237
ClinVar RCV Id: RCV001173941 RCV003744737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Pro725Ser
CA405896842
NM_181882.3:c.2173C>T