Canonical Allele Identifier: PA2827982935
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 937461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln386His
CA16024227
NM_001354900.2:c.1158G>C
CA16024228
NM_001354900.2:c.1158G>T