ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA658818957
Gene: VPS33B
HGNC
NCBI
Linked Data
ClinVar Variation Id:
499620
ClinVar RCV Id:
RCV000591538
RCV000765242
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_061138.3:p.Ser562Asn
CA7744540
NM_018668.5:c.1685G>A