Canonical Allele Identifier: PA121976
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 12219
ClinVar RCV Id: RCV000013003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Pro7Leu
CA121974
NM_000490.5:c.20C>T