Canonical Allele Identifier: PA2827990665
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216188
ClinVar RCV Id: RCV000196318 RCV000478701 RCV000567493 RCV000779724 RCV000765792 RCV002228917 RCV003996983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp2780Gly
CA050869
NM_001354900.2:c.8339A>G