Canonical Allele Identifier: PA2827964680
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 937461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln420His
CA16024227
NM_001354898.2:c.1260G>C
CA16024228
NM_001354898.2:c.1260G>T