Canonical Allele Identifier: PA096812
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2339
ClinVar RCV Id: RCV000002429 RCV000523135 RCV001290020 RCV002444414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Tyr293Cys
CA281524
NM_130468.4:c.878A>G