Canonical Allele Identifier: PA2827999385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met2654Thr
CA16039005
NM_001354901.2:c.7961T>C