Canonical Allele Identifier: PA2825191903
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 3236029
ClinVar RCV Id: RCV004555290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Cys110Ser
CA408061435
NM_000490.5:c.329G>C
CA408061438
NM_000490.5:c.328T>A