Canonical Allele Identifier: PA2580300158
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1964696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Trp168Arg
CA224164933
NM_003977.4:c.502T>C
CA381550458
NM_003977.4:c.502T>A