Canonical Allele Identifier: PA645462701
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411990
ClinVar RCV Id: RCV000471372 RCV000663198 RCV001013302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro61Ser
CA16611261
NM_000551.4:c.181C>T