Canonical Allele Identifier: PA2499265263
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1035289
ClinVar RCV Id: RCV001338136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Gly57Ser
CA381546724
NM_003977.4:c.169G>A