Canonical Allele Identifier: PA2825313777
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2051085
ClinVar RCV Id: RCV002922270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Asn17Asp
CA5589335
NM_001015880.2:c.49A>G