Allele Registry

Canonical Allele Identifier: PA658654715

Gene: CHST14 HGNC NCBI

ClinVar Variation Id: 440975

HGVS (amino-acid)	Matching Registered Transcripts
NP_569735.1:p.Arg345Trp	CA7481690 NM_130468.4:c.1033C>T