Canonical Allele Identifier: PA2827982931
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His385Arg
CA004248
NM_001354900.2:c.1154A>G