Allele Registry

Canonical Allele Identifier: PA2825661357

Gene: CHST8 HGNC NCBI

ClinVar RCV:

RCV000162277

RCV000890550

RCV003917553

ClinVar Variation:

183645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121368.1:p.Arg77Trp	CA186116 NM_001127896.1:c.229C>T