This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2825313775
Gene: PAPSS2 HGNC NCBI
ClinVar RCV:
RCV002814788
ClinVar Variation:
1998630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Gln12Arg
CA377485143
NM_001015880.2:c.35A>G