Canonical Allele Identifier: PA2580300142
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1782653
ClinVar RCV Id: RCV002410686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ile64Thr
CA6140749
NM_003977.4:c.191T>C