Canonical Allele Identifier: PA107962
Gene: CHST6 HGNC NCBI
ClinVar RCV:
RCV000005376
ClinVar Variation:
5072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Asp203Glu
CA250519
NM_021615.5:c.609C>A
CA396790633
NM_021615.5:c.609C>G