Canonical Allele Identifier: PA2573205655
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1442097
ClinVar RCV Id: RCV001969786
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Thr164Ser
CA1345067419
NM_001354723.2:c.491C>G
CA2573332051
NM_001354723.2:c.490A>T