Canonical Allele Identifier: PA2827989925
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2555Ala
CA014059
NM_001354900.2:c.7663T>G