Canonical Allele Identifier: PA2826875221
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1360852
ClinVar RCV Id: RCV001907226 RCV002425130
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Val13Leu
CA6140752
NM_001302959.2:c.37G>C
CA381547025
NM_001302959.2:c.37G>T