Canonical Allele Identifier: PA2826876062
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1964696
ClinVar RCV Id: RCV002721556 RCV003348900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Trp168Arg
CA224164933
NM_001302960.2:c.502T>C
CA381550458
NM_001302960.2:c.502T>A