Canonical Allele Identifier: PA156892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133539
ClinVar RCV Id: RCV000120050 RCV000196705 RCV000589545 RCV000216893 RCV003315720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu129Gln
CA008713
NM_001127510.3:c.385G>C