Canonical Allele Identifier: PA344178
Gene: AIP HGNC NCBI
ClinVar Allele:
49624
ClinVar RCV:
RCV000034101
ClinVar Variation:
41202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Tyr248del
CA344175
NM_003977.4:c.742_744del