Canonical Allele Identifier: PA2826875767
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1499310
ClinVar RCV Id: RCV002010575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly31Arg
CA381545883
NM_001302960.2:c.91G>A
CA381545885
NM_001302960.2:c.91G>C