Canonical Allele Identifier: PA2827983547
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1478972
ClinVar RCV Id: RCV002579516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His611Pro
CA16025590
NM_001354900.2:c.1832A>C