Canonical Allele Identifier: PA253732
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 6047
ClinVar RCV Id: RCV000006419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Leu286Pro
CA253731
NM_004273.5:c.857T>C