Canonical Allele Identifier: PA163848
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1352Ala
CA008875
NM_000038.6:c.4055T>C