Canonical Allele Identifier: PA294157
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1493Met
CA009574
NM_001127510.3:c.4478C>T