Canonical Allele Identifier: PA2499235192
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044571
ClinVar RCV Id: RCV001348833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Ala336Val
CA377489532
NM_001015880.2:c.1007C>T