Canonical Allele Identifier: PA2829557255
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Gly433Asp
CA377483043
NM_004670.4:c.1298G>A