Allele Registry

Canonical Allele Identifier: PA645392972

Gene: CHST14 HGNC NCBI

ClinVar Allele:

271609

ClinVar RCV:

RCV000268389

RCV001270131

RCV004021221

ClinVar Variation:

287372

HGVS (amino-acid)	Matching Registered Transcripts
NP_569735.1:p.Arg314Gln	CA7481671 NM_130468.4:c.941G>A