Canonical Allele Identifier: PA1139740017
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 936379
ClinVar RCV Id: RCV002348668 RCV003650670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1785Ala
CA16032919
NM_001354896.2:c.5354G>C