Canonical Allele Identifier: PA253738
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 6050
ClinVar RCV Id: RCV000006422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Leu161Phe
CA253737
NM_004273.5:c.481C>T