Canonical Allele Identifier: PA118419
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_001015880.1:p.Thr48Arg
CA118418
NM_001015880.2:c.143C>G