Canonical Allele Identifier: PA2742021687
Gene: SULT2B1 HGNC NCBI
ClinVar RCV:
RCV003722023
ClinVar Variation:
2883545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_814444.1:p.Arg198Trp
CA309387084
NM_177973.1:c.592C>T