Canonical Allele Identifier: PA2827976974
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135701
ClinVar RCV Id: RCV000122779 RCV000235379 RCV001193569 RCV000575531 RCV003997378 RCV003743579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile1389Leu
CA009397
NM_001354899.2:c.4165A>C