Canonical Allele Identifier: PA2826875563
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 485056
ClinVar RCV Id: RCV000573085 RCV000765006 RCV001202575 RCV003465251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ala217Val
CA6140987
NM_001302959.2:c.650C>T