Canonical Allele Identifier: PA2828022553
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile1471Phe
CA039634
NM_001354903.2:c.4411A>T