Canonical Allele Identifier: PA2826875312
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1432094
ClinVar RCV Id: RCV001941094 RCV003303441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ser100Arg
CA381550256
NM_001302959.2:c.298A>C
CA381550278
NM_001302959.2:c.300C>A
CA381550279
NM_001302959.2:c.300C>G