Canonical Allele Identifier: PA2826875427
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2489486
ClinVar RCV Id: RCV004277809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Met155Thr
CA381551373
NM_001302959.2:c.464T>C