Canonical Allele Identifier: PA2828026851
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile2130Phe
CA012398
NM_001354903.2:c.6388A>T