Canonical Allele Identifier: PA2825190695
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_000542.1:p.Glu42Asp
CA351747990
NM_000551.4:c.126G>C
CA351747994
NM_000551.4:c.126G>T