Canonical Allele Identifier: PA2825636067
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 801041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2580Ala
CA16038136
NM_001127510.3:c.7738T>G