Canonical Allele Identifier: PA916040476
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1688Val
CA009818
NM_001354896.2:c.5063C>T