Canonical Allele Identifier: PA2827961802
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln2386His
CA047019
NM_001354897.2:c.7158G>C
CA16036857
NM_001354897.2:c.7158G>T