Canonical Allele Identifier: PA2828026480
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Met1930Ile
CA012330
NM_001354906.2:c.5790G>A
CA16035852
NM_001354906.2:c.5790G>C
CA16035853
NM_001354906.2:c.5790G>T