Canonical Allele Identifier: PA658660026
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1572Phe
CA039634
NM_001127510.3:c.4714A>T