Canonical Allele Identifier: PA2580300133
Gene: AIP HGNC NCBI
ClinVar RCV:
RCV002850986
ClinVar Variation:
2010264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asp51Gly
CA381546623
NM_003977.4:c.152A>G