Canonical Allele Identifier: PA2573175977
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490855
ClinVar RCV Id: RCV001986093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Cys355Ser
CA377489655
NM_001015880.2:c.1063T>A
CA377489657
NM_001015880.2:c.1064G>C