ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA891853843
Gene: VHL
HGNC
NCBI
Linked Data
ClinVar Variation Id:
574321
ClinVar RCV Id:
RCV000696229
RCV002334321
RCV000997984
RCV003999652
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000542.1:p.Pro2Ser
CA70042126
NM_000551.4:c.4C>T