Canonical Allele Identifier: PA215521
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu150Asp
CA008951
NM_001127511.3:c.450G>C
CA16022242
NM_001127511.3:c.450G>T