Canonical Allele Identifier: PA097292
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 6687
ClinVar RCV Id: RCV000007075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Thr48Arg
CA118418
NM_004670.4:c.143C>G