Canonical Allele Identifier: PA2828010553
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile2071Phe
CA012398
NM_001354905.2:c.6211A>T