Canonical Allele Identifier: PA916040602
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356
ClinVar RCV Id: RCV000566944 RCV001800683 RCV003492060 RCV004001918 RCV003401490 RCV003766558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys1788Glu
CA041323
NM_001354896.2:c.5362A>G