Canonical Allele Identifier: PA913198703
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 593375
ClinVar RCV Id: RCV000728398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Gly413Cys
CA377151823
NM_004273.5:c.1237G>T