Allele Registry

Canonical Allele Identifier: PA096781

Gene: CHST14 HGNC NCBI

ClinVar Allele:

17381

ClinVar RCV:

RCV000002432

ClinVar Variation:

2342

HGVS (amino-acid)	Matching Registered Transcripts
NP_569735.1:p.Cys289Ser	CA281531 NM_130468.4:c.866G>C CA391767623 NM_130468.4:c.865T>A