Canonical Allele Identifier: PA2827947712
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2555Pro
CA16037980
NM_001354895.2:c.7663T>C