Canonical Allele Identifier: PA916041946
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala450Thr
CA16024191
NM_001354897.2:c.1348G>A