Canonical Allele Identifier: PA2828023355
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1588Ile
CA040566
NM_001354903.2:c.4763C>T