Canonical Allele Identifier: PA2829557202
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2140719
ClinVar RCV Id: RCV003056593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Arg341Cys
CA5589628
NM_004670.4:c.1021C>T