Canonical Allele Identifier: PA2827971037
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln2378Pro
CA10578440
NM_001354898.2:c.7133A>C