Allele Registry

Canonical Allele Identifier: PA645392965

Gene: CHST14 HGNC NCBI

ClinVar Allele:

360186

ClinVar RCV:

RCV000414071

RCV000585577

RCV001086290

RCV002278648

RCV002365452

ClinVar Variation:

373593

HGVS (amino-acid)	Matching Registered Transcripts
NP_569735.1:p.Val212Ala	CA7481625 NM_130468.4:c.635T>C