Canonical Allele Identifier: PA645392967
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 434766
ClinVar RCV Id: RCV000500082 RCV001561424 RCV002271341 RCV003962376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Glu262Lys
CA391767055
NM_130468.4:c.784G>A