Canonical Allele Identifier: PA096781
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2342
ClinVar RCV Id: RCV000002432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Cys289Ser
CA281531
NM_130468.4:c.866G>C
CA391767623
NM_130468.4:c.865T>A