Canonical Allele Identifier: PA645462958
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 418539
ClinVar RCV Id: RCV000479431 RCV001036041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala122Ser
CA16617788
NM_000551.4:c.364G>T