Canonical Allele Identifier: PA2580556358
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2451973
ClinVar RCV Id: RCV003187669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu42Asp
CA351747990
NM_198156.3:c.126G>C
CA351747994
NM_198156.3:c.126G>T