Canonical Allele Identifier: PA2826875309
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 3223615
ClinVar RCV Id: RCV004516379
ClinVar Variation Id: 3223616
ClinVar RCV Id: RCV004516380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Val98Leu
CA381550224
NM_001302959.2:c.292G>T
CA381550226
NM_001302959.2:c.292G>C