Canonical Allele Identifier: PA2829557181
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442969
ClinVar RCV Id: RCV001960403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Gly312Val
CA211271747
NM_004670.4:c.935G>T