ClinGen Allele Registry
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Canonical Allele Identifier:
PA916056976
Gene: VHL
HGNC
NCBI
Linked Data
ClinVar Variation Id:
418538
ClinVar RCV Id:
RCV000696976
RCV001294070
RCV001018619
RCV001712442
RCV003900013
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_937799.1:p.Gly30Glu
CA16617781
NM_198156.3:c.89G>A