Canonical Allele Identifier: PA2825313870
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3208526
ClinVar RCV Id: RCV004502422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Ile297Met
CA5589604
NM_001015880.2:c.891C>G