Canonical Allele Identifier: PA2826875753
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2452494
ClinVar RCV Id: RCV003172588
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Asp27Glu
CA381545859
NM_001302960.2:c.81C>A
CA381545860
NM_001302960.2:c.81C>G