Canonical Allele Identifier: PA2827968319
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile1547Phe
CA039634
NM_001354898.2:c.4639A>T