ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829557168
Gene: PAPSS2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1022650
ClinVar RCV Id:
RCV001322588
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004661.2:p.Gly290Ser
CA5589600
NM_004670.4:c.868G>A