Canonical Allele Identifier: PA2826876285
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2031572
ClinVar RCV Id: RCV002867313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ter284Arg
CA475509537
NM_001302960.2:c.850T>C
CA475509538
NM_001302960.2:c.850T>A