Canonical Allele Identifier: PA1139734355
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 962288
ClinVar RCV Id: RCV001236119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val119Leu
CA1139655731
NM_001354723.2:c.355G>C
CA2664401523
NM_001354723.2:c.355G>T