Canonical Allele Identifier: PA2827940857
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1494734
ClinVar RCV Id: RCV003773269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ile446Thr
CA16024233
NM_001354895.2:c.1337T>C