Canonical Allele Identifier: PA2825640297
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gln1175Arg
CA16029193
NM_001127511.3:c.3524A>G