Canonical Allele Identifier: PA2580505310
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775451
ClinVar RCV Id: RCV002405604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Gln349Leu
CA391768783
NM_130468.4:c.1046A>T