Canonical Allele Identifier: PA2828029635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761661
ClinVar RCV Id: RCV002419234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly2389Ala
CA16038742
NM_001354906.2:c.7166G>C