Canonical Allele Identifier: PA2742021687
Gene: SULT2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2883545
ClinVar RCV Id: RCV003722023

Amino-acid Alleles

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