Canonical Allele Identifier: PA2827926519
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1052300
ClinVar RCV Id: RCV001360453 RCV001773713 RCV002341754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu17Asp
CA351747259
NM_001354723.2:c.51G>C
CA351747262
NM_001354723.2:c.51G>T