Canonical Allele Identifier: PA2573232117
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1449487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Glu192Gly
CA6140875
NM_003977.4:c.575A>G