Canonical Allele Identifier: PA2580300134
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1774401
ClinVar RCV Id: RCV002392403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asp51His
CA381546617
NM_003977.4:c.151G>C