Canonical Allele Identifier: PA2827973835
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His416Arg
CA004248
NM_001354899.2:c.1247A>G