Canonical Allele Identifier: PA2828019037
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2774891
ClinVar RCV Id: RCV003586071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro923Ala
CA16028057
NM_001354903.2:c.2767C>G