Canonical Allele Identifier: PA2580300159
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2452491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Met170Ile
CA381550500
NM_003977.4:c.510G>A
CA381550501
NM_003977.4:c.510G>C
CA381550503
NM_003977.4:c.510G>T