Canonical Allele Identifier: PA2827947710
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2555Ala
CA16037981
NM_001354895.2:c.7663T>G