Canonical Allele Identifier: PA2829557187
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2200342
ClinVar RCV Id: RCV002638168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Arg323Trp
CA5589619
NM_004670.4:c.967C>T