Canonical Allele Identifier: PA2825191269
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2934338
ClinVar RCV Id: RCV003796088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro103Ser
CA351751072
NM_000551.4:c.307C>T