Canonical Allele Identifier: PA2741906431
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_003968.3:p.Lys215Asn
CA381551403
NM_003977.4:c.645G>C
CA381551405
NM_003977.4:c.645G>T