Canonical Allele Identifier: PA2826876099
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 957874
ClinVar RCV Id: RCV001230940 RCV002348776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Glu185Lys
CA224165001
NM_001302960.2:c.553G>A