Canonical Allele Identifier: PA2830430887
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 135407
ClinVar RCV Id: RCV000122261 RCV001038969 RCV003162559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu145Asp
CA020484
NM_198156.3:c.435A>C
CA351756388
NM_198156.3:c.435A>T