Canonical Allele Identifier: PA093117
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 12212
ClinVar RCV Id: RCV000012996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Ala19Val
CA121959
NM_000490.5:c.56C>T