Canonical Allele Identifier: PA2826875573
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2813549
ClinVar RCV Id: RCV003680497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Asn221Ser
CA381554722
NM_001302959.2:c.662A>G