Canonical Allele Identifier: PA2828052377
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val282Asp
CA16024206
NM_001354905.2:c.845T>A