Canonical Allele Identifier: PA2573232062
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1425200
ClinVar RCV Id: RCV001924342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ile85Thr
CA381547273
NM_003977.4:c.254T>C