Allele Registry

Canonical Allele Identifier: PA103311

Gene: CHST8 HGNC NCBI

ClinVar RCV:

RCV000162277

RCV000890550

RCV003917553

ClinVar Variation:

183645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121367.1:p.Arg77Trp	CA186116 NM_001127895.1:c.229C>T