Canonical Allele Identifier: PA1139714235
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 954536
ClinVar RCV Id: RCV001227005 RCV002255634 RCV003469398
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Leu25Phe
CA6140676
NM_003977.4:c.73C>T