Canonical Allele Identifier: PA1139688403
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 855703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Met68Ile
CA6140794
NM_001302959.2:c.204G>A
CA381549434
NM_001302959.2:c.204G>C
CA381549436
NM_001302959.2:c.204G>T