Canonical Allele Identifier: PA2825644213
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 658256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2441Cys
CA16037401
NM_001127511.3:c.7322C>G