Canonical Allele Identifier: PA658660830
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2615Thr
CA16038374
NM_001127510.3:c.7844T>C