Canonical Allele Identifier: PA2828003726
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile2140Phe
CA012398
NM_001354902.2:c.6418A>T