Canonical Allele Identifier: PA2829557358
Gene: PAPSS2 HGNC NCBI
ClinVar RCV:
RCV002733167
ClinVar Variation:
2245740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004661.2:p.Phe595Ser
CA211241648
NM_004670.4:c.1784T>C