Canonical Allele Identifier: PA916040518
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1720Arg
CA10578394
NM_001354896.2:c.5158G>A
CA16032490
NM_001354896.2:c.5158G>C