Canonical Allele Identifier: PA2827997770
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2172Phe
CA012398
NM_001354901.2:c.6514A>T