Canonical Allele Identifier: PA2825644476
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 579380
ClinVar RCV Id: RCV003534706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Trp2529Arg
CA16037921
NM_001127511.3:c.7585T>A
CA16037922
NM_001127511.3:c.7585T>C