Canonical Allele Identifier: PA916042505
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp978His
CA008365
NM_001354905.2:c.2932G>C