Canonical Allele Identifier: PA1139680019
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 976038
ClinVar RCV Id: RCV001253211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Glu78del
CA408061656
NM_000490.5:c.232G>T
CA408061662
NM_000490.5:c.229G>T
CA2346405565
NM_000490.5:c.232_234del