Canonical Allele Identifier: PA2826875514
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1759691
ClinVar RCV Id: RCV002394191 RCV003099694
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.His194Gln
CA6140930
NM_001302959.2:c.582C>G
CA381551897
NM_001302959.2:c.582C>A