Canonical Allele Identifier: PA2827948243
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Met2713Thr
CA16039005
NM_001354895.2:c.8138T>C