Canonical Allele Identifier: PA658677083
Gene: CHST3 HGNC NCBI
ClinVar RCV:
RCV000550153
ClinVar Variation:
478822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Asp302His
CA377147897
NM_004273.5:c.904G>C