Canonical Allele Identifier: PA916041522
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2559Val
CA013946
NM_001354896.2:c.7675A>G