Canonical Allele Identifier: PA2828002522
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1488Phe
CA10584253
NM_001354902.2:c.4462A>T