Canonical Allele Identifier: PA2826875867
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1360852
ClinVar RCV Id: RCV001907226 RCV002425130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Val72Leu
CA6140752
NM_001302960.2:c.214G>C
CA381547025
NM_001302960.2:c.214G>T