Canonical Allele Identifier: PA16040150
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2686Ala
CA049793
NM_000038.6:c.8057T>C