Canonical Allele Identifier: PA2829557212
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490855
ClinVar RCV Id: RCV001986093
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Cys350Ser
CA377489655
NM_004670.4:c.1048T>A
CA377489657
NM_004670.4:c.1049G>C