Canonical Allele Identifier: PA2826875741
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 485057
ClinVar RCV Id: RCV000576100 RCV000914288
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Glu24Asp
CA6140675
NM_001302960.2:c.72G>C
CA381545842
NM_001302960.2:c.72G>T