Canonical Allele Identifier: PA2827971620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 801041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2555Ala
CA16038136
NM_001354898.2:c.7663T>G