Canonical Allele Identifier: PA108105
Gene: CHST6 HGNC NCBI
ClinVar RCV:
RCV000005375
ClinVar Variation:
5071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Lys174Arg
CA250518
NM_021615.5:c.521A>G