Allele Registry

Canonical Allele Identifier: PA096812

Gene: CHST14 HGNC NCBI

ClinVar RCV:

RCV000002429

RCV000523135

RCV001290020

RCV002444414

ClinVar Variation:

2339

HGVS (amino-acid)	Matching Registered Transcripts
NP_569735.1:p.Tyr293Cys	CA281524 NM_130468.4:c.878A>G