Canonical Allele Identifier: PA2573175971
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1464080
ClinVar RCV Id: RCV001961270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Leu305Arg
CA377489343
NM_001015880.2:c.914T>G