Canonical Allele Identifier: PA2826875429
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2719391
ClinVar RCV Id: RCV003553624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Lys156Asn
CA381551403
NM_001302959.2:c.468G>C
CA381551405
NM_001302959.2:c.468G>T