Canonical Allele Identifier: PA1139732754
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 937461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln455His
CA16024227
NM_001354897.2:c.1365G>C
CA16024228
NM_001354897.2:c.1365G>T