Canonical Allele Identifier: PA2825644601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys2567Thr
CA10578450
NM_001127511.3:c.7700A>C