Canonical Allele Identifier: PA2828036428
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1315725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp890Tyr
CA16028002
NM_001354904.2:c.2668G>T