Canonical Allele Identifier: PA2825020844
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile1572Phe
CA039634
NM_000038.6:c.4714A>T