Canonical Allele Identifier: PA2826875550
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41210
ClinVar RCV Id: RCV000034109 RCV001852690 RCV002415456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Arg212Trp
CA344201
NM_001302959.2:c.634C>T