Canonical Allele Identifier: PA2829553118
Gene: SULT2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378138
ClinVar RCV Id: RCV001880996
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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