Canonical Allele Identifier: PA2829557174
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3208526
ClinVar RCV Id: RCV004502422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Ile292Met
CA5589604
NM_004670.4:c.876C>G