Canonical Allele Identifier: PA2828052356
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala280Thr
CA16024191
NM_001354905.2:c.838G>A