Canonical Allele Identifier: PA2742006968
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2778855
ClinVar RCV Id: RCV003633769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Arg29Gly
CA391762135
NM_130468.4:c.85A>G