Canonical Allele Identifier: PA2580131968
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165979
ClinVar RCV Id: RCV003090258 RCV003090257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Gly438Asp
CA377483043
NM_001015880.2:c.1313G>A