Canonical Allele Identifier: PA2828032237
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2105910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr285Ser
CA16023339
NM_001354904.2:c.853A>T
CA16023341
NM_001354904.2:c.854C>G