Canonical Allele Identifier: PA2827997428
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala2069Val
CA044469
NM_001354901.2:c.6206C>T