ClinGen Allele Registry
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Canonical Allele Identifier:
PA645392972
Gene: CHST14
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
271609
ClinVar RCV:
RCV000268389
RCV001270131
RCV004021221
ClinVar Variation:
287372
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_569735.1:p.Arg314Gln
CA7481671
NM_130468.4:c.941G>A