Canonical Allele Identifier: PA2828030062
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Met2612Thr
CA16039005
NM_001354903.2:c.7835T>C