Canonical Allele Identifier: PA2826876040
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1432094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ser159Arg
CA381550256
NM_001302960.2:c.475A>C
CA381550278
NM_001302960.2:c.477C>A
CA381550279
NM_001302960.2:c.477C>G