ClinGen Allele Registry
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Canonical Allele Identifier:
PA108813
Gene: ST3GAL3
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000023551
ClinVar Variation:
30587
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_006270.1:p.Ala13Asp
CA129359
NM_006279.4:c.38C>A