Canonical Allele Identifier: PA2827942986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Val1125Ala
CA008333
NM_001354895.2:c.3374T>C