Canonical Allele Identifier: PA2827926620
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1757751
ClinVar RCV Id: RCV002370945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu41Asp
CA351747945
NM_001354723.2:c.123A>T
CA351747951
NM_001354723.2:c.123A>C