Canonical Allele Identifier: PA2826875605
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41214
ClinVar RCV Id: RCV000034113 RCV000571818 RCV001357152 RCV003904890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ala240Val
CA344210
NM_001302959.2:c.719C>T