Allele Registry

Canonical Allele Identifier: PA284653

Gene: CHST14 HGNC NCBI

ClinVar RCV:

RCV000043688

ClinVar Variation:

50992

HGVS (amino-acid)	Matching Registered Transcripts
NP_569735.1:p.Arg274Pro	CA284651 NM_130468.4:c.821G>C