Canonical Allele Identifier: PA2826875216
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 820621
ClinVar RCV Id: RCV001014268 RCV001043193 RCV003153884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Lys10Glu
CA6140751
NM_001302959.2:c.28A>G