Canonical Allele Identifier: PA916039683
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 83212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile656Val
CA006325
NM_001354896.2:c.1966A>G