Canonical Allele Identifier: PA2828013479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val2526Ala
CA049793
NM_001354905.2:c.7577T>C