Canonical Allele Identifier: PA2825024894
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2611Lys
CA049276
NM_000038.6:c.7832C>A