Canonical Allele Identifier: PA2827996516
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1784Thr
CA16033423
NM_001354901.2:c.5350C>A