Canonical Allele Identifier: PA2828029690
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2751906
ClinVar RCV Id: RCV003536738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro2564Arg
CA16038697
NM_001354903.2:c.7691C>G