Canonical Allele Identifier: PA2580304965
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133077
ClinVar RCV Id: RCV003056201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Gln402Glu
CA377151669
NM_004273.5:c.1204C>G