Canonical Allele Identifier: PA2829553118
Gene: SULT2B1 HGNC NCBI
ClinVar RCV:
RCV001880996
ClinVar Variation:
1378138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004596.2:p.Leu318Pro
CA406715302
NM_004605.2:c.953T>C