Canonical Allele Identifier: PA2826876262
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1761972
ClinVar RCV Id: RCV002419457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gln267His
CA381554460
NM_001302960.2:c.801A>C
CA381554467
NM_001302960.2:c.801A>T