ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826876206
Gene: AIP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
49619
ClinVar RCV:
RCV000034096
RCV001379496
RCV004018729
ClinVar Variation:
41197
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001289889.1:p.Cys238Tyr
CA344155
NM_001302960.2:c.713G>A