Canonical Allele Identifier: PA2828049303
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met2587Thr
CA16039005
NM_001354904.2:c.7760T>C