ClinGen Allele Registry
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Canonical Allele Identifier:
PA916019373
Gene: AIP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
49598
ClinVar RCV:
RCV000034075
RCV001021265
RCV001052633
ClinVar Variation:
41176
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001289888.1:p.Arg69His
CA344099
NM_001302959.2:c.206G>A