Canonical Allele Identifier: PA2825024754
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2576Thr
CA16038108
NM_000038.6:c.7726G>A