Canonical Allele Identifier: PA2826875756
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2452485
ClinVar RCV Id: RCV003172579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Phe28Leu
CA381545862
NM_001302960.2:c.82T>C
CA381545867
NM_001302960.2:c.84T>A
CA381545868
NM_001302960.2:c.84T>G