Canonical Allele Identifier: PA2826876146
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 485073
ClinVar RCV Id: RCV000572851 RCV001326482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ala207Thr
CA381551218
NM_001302960.2:c.619G>A