Canonical Allele Identifier: PA2827988707
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2190Phe
CA012398
NM_001354900.2:c.6568A>T