Canonical Allele Identifier: PA2827980629
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2503Ala
CA16037824
NM_001354899.2:c.7507T>G