Allele Registry

Canonical Allele Identifier: PA096776

Gene: CHST14 HGNC NCBI

ClinVar RCV:

RCV000002427

RCV001290021

ClinVar Variation:

2337

HGVS (amino-acid)	Matching Registered Transcripts
NP_569735.1:p.Arg213Pro	CA281522 NM_130468.4:c.638G>C