ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829477270
Gene: AIP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
49585
ClinVar RCV:
RCV000034062
RCV001852688
ClinVar Variation:
41163
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003968.3:p.Gly47_Arg54del
CA344059
NM_003977.4:c.140_163del