Canonical Allele Identifier: PA093351
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 12214
ClinVar RCV Id: RCV000012998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Gly54Arg
CA121963
NM_000490.5:c.160G>C
CA408061811
NM_000490.5:c.160G>A