Canonical Allele Identifier: PA111733
Gene: PRRX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29825
ClinVar RCV Id: RCV000022701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073207.1:p.Phe113Ser
CA259669
NM_022716.4:c.338T>C