Canonical Allele Identifier: PA2580131960
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_001015880.1:p.Arg328Trp
CA5589619
NM_001015880.2:c.982C>T