Canonical Allele Identifier: PA2827968733
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1677Arg
CA10578394
NM_001354898.2:c.5029G>A
CA16032490
NM_001354898.2:c.5029G>C