Canonical Allele Identifier: PA2499266585
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052360
ClinVar RCV Id: RCV001360522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Asp327Ala
CA209479313
NM_004273.5:c.980A>C