Canonical Allele Identifier: PA168372
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142442
ClinVar RCV Id: RCV000131566 RCV000229880 RCV000478677 RCV000656752 RCV003315910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2596Ala
CA014059
NM_001127510.3:c.7786T>G