Allele Registry

Canonical Allele Identifier: PA253732

Gene: CHST3 HGNC NCBI

ClinVar Allele:

21086

ClinVar RCV:

RCV000006419

ClinVar Variation:

6047

HGVS (amino-acid)	Matching Registered Transcripts
NP_004264.2:p.Leu286Pro	CA253731 NM_004273.5:c.857T>C