Canonical Allele Identifier: PA658677079
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 478823
ClinVar RCV Id: RCV000528005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Pro164Leu
CA377144138
NM_004273.5:c.491C>T