Canonical Allele Identifier: PA2825190437
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1002447
ClinVar RCV Id: RCV001298878 RCV002418901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asn7Ser
CA351747048
NM_000551.4:c.20A>G