Canonical Allele Identifier: PA2741825314
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2918559
ClinVar RCV Id: RCV003619121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Arg349Cys
CA377489618
NM_001015880.2:c.1045C>T