Canonical Allele Identifier: PA645392958
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 281584
ClinVar RCV Id: RCV000724922 RCV001859550 RCV002392794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Ala48Val
CA7481552
NM_130468.4:c.143C>T