Canonical Allele Identifier: PA2827989813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1410428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2520Gly
CA16038016
NM_001354900.2:c.7559T>G