Canonical Allele Identifier: PA2826876138
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 861318
ClinVar RCV Id: RCV001067823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Asp204Gly
CA381551167
NM_001302960.2:c.611A>G